US4654462AExpiredUtility
Metathesis of olefins with a catalyst based upon a tungsten complex
Est. expiryFeb 12, 2005(expired)· nominal 20-yr term from priority
B01J 31/34B01J 2531/66B01J 31/2226C07C 2531/22C07C 6/04B01J 31/0214C07C 2531/14B01J 31/2265B01J 2231/543C07C 2531/12B01J 31/122
65
PatentIndex Score
20
Cited by
16
References
17
Claims
Abstract
Improved process of metathesis of olefins by contact of one or more olefins with a catalyst comprising a tungsten complex with two phenoxy groups, carrying substituents and four other ligands, the complex carrying as coordination groups a halogen atom, an alkyl radical and a carbene. The catalyst preferably is of the formula <IMAGE> where X is halogen, R is hydrocarbon or an electronegative group or atom, R1 is alkyl and R2 and R3 are individually hydrogen or alkyl groups.
Claims
exact text as granted — not AI-modifiedWe claim:
1. Improved process for the metathesis of olefins comprising contact of at least one olefin with a catalyst characterised in that the catalyst is of the formula ##STR19## where X is a halogen, R is a hydrocarbon group or an electronegative group or atom, R 1 is an alkyl group, and R 2 and R 3 individually are hydrogen atoms or straight or branched C 1 to C 8 alkyl groups.
2. Process according to claim 1, characterized in that at least one molecule of an ether R 4 --O--R 4 is complexed in the catalyst, R 4 being a C 2 to C 6 alkyl.
3. Process according to claim 2 wherein R 4 is ethyl or isopropyl.
4. Process according to claim 1, characterised in that at least one molecule of dioxane or an ether ##STR20## is complexed in the catalyst, where n is an integer of 0 to 6 and m=1.
5. Process according to claim 1, characterized in that the catalyst is employed without any co-catalyst between 0° and 100° C. and the proportion of olefin is from 30 to 300 moles per atom of W present.
6. Process according to claim 5 wherein said temperature is 50°-95° C. and the proportion of olefin is 50-150 moles per atom of W present.
7. Process according to claim 1 characterised in that the catalyst is employed with a Lewis acid co-catalyst.
8. Process according to claim 7 characterized in that said co-catalyst is an organo aluminum, tin, lead, magnesium or titanium compound Lewis acid.
9. Process according to claim 1 wherein R 1 is a C 1-8 alkyl group.
10. Process according to claim 1 characterized in that R is phenyl, methyl, Cl or F, R 1 is neopentyl, R 2 is tert-butyl, R 3 is hydrogen and said catalyst contains complexed therein at least one molecule of diethyl ether or diisopropyl ether.
11. Catalyst for carrying out the metathesis comprising a diphenoxy tungsten complex, characterised by the structure ##STR21## where X is a halogen, R is a hydrocarbon group or an electro-negative group or atom, R 1 is an alkyl group, and R 2 and R 3 individually are hydrogen atoms or straight or branched C 1 to C 8 alkyl groups.
12. Catalyst according to claim 11, characterised in that a mole of ether R 4 OR 4 or ##STR22## is combined with the molecule of the complex, R 4 being a C 2 to C 6 alkyl, n being 0 to 6 and m=1 or 2.
13. Catalyst according to claim 11, characterised in that R is phenyl, methyl, Cl or F R 1 is a neopentyl, R 2 is a tert-butyl and R 3 is a hydrogen atom.
14. Catalyst according to claim 12, characterised in that R 4 is ethyl or an isopropyl.
15. Process of preparation of a complex catalyst according to claim 11, characterised in that Mg(CHR'R") 2 wherein R' and R" are H or alkyl is reacted with a tetra-halogeno complex of di-phenoxy tungsten ##STR23## in an ether.
16. Catalyst according to claim 11 wherein R 1 is C 1-8 alkyl.
17. Catalyst according to claim 13 characterized in that a mole of diethyl ether or diisopropyl ether is combined with the molecule of the diphenoxy tungsten complex.Cited by (0)
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